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Clinical Trial Summary

1. to investigate the association between route of administration of exogenous estrogen (transdermal vs. oral) and cardiorenal risk in cisgender (gender identity aligning with sex at birth) and transgender (gender identity not aligning with sex at birth) women. 2. to investigate the association between exogenous testosterone exposure and cardiorenal risk in cisgender (gender identity aligning with sex at birth) and transgender (gender identity not aligning with sex at birth) men.


Clinical Trial Description

Participants are screened for eligibility. Study involves a 4.5 hour morning in the lab: 1. Participants come fasting 2. IV infusion and blood draws 3. Non invasive testing - Holter monitor, sphygmocor, bioelectrical impedance, blood pressure checks ;


Study Design


Related Conditions & MeSH terms


NCT number NCT05442463
Study type Observational
Source University of Calgary
Contact Darlene Y Sola, BScN
Phone 4032107434
Email dsola@ucalgary.ca
Status Recruiting
Phase
Start date November 30, 2020
Completion date November 30, 2025

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